Different vitamin K forms in hemodialysis patients: a simple dietary supplement to battle vascular calcification—randomized controlled trial

Background and aim Vascular calcification is a significant risk factor for cardiovascular diseases in patients with end-stage renal disease, particularly those on hemodialysis. Previous research on vitamin K found that it had a positive on calcification markers. However, clinical data is still limit...

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Published inThe Egyptian journal of internal medicine Vol. 35; no. 1; pp. 4 - 7
Main Authors Elshinnawy, Howaida Abdelhameed, El-Said, Tamer Wahid, Fahmy, Sarah Farid, Shamseldin, Ahmed, Ibrahim, Sherin, Elsharabasy, Reem Mohsen
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 23.01.2023
Springer Nature B.V
SpringerOpen
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Summary:Background and aim Vascular calcification is a significant risk factor for cardiovascular diseases in patients with end-stage renal disease, particularly those on hemodialysis. Previous research on vitamin K found that it had a positive on calcification markers. However, clinical data is still limited. This study aimed to compare the efficacy and safety of vitamin K2 versus vitamin k1 on a calcification regulator in hemodialysis patients. Methods A prospective randomized placebo-controlled trial was conducted on 120 patients, who were divided into three groups; group 1: administered 10 mg of vitamin K1 (phytomenadione thrice weekly); group 2: administered 90 μg of vitamin k2 (MK-7); group 3: administered placebo for 3 months. Matrix Gla protein (MGP), calcium, phosphorous, and intact parathyroid hormone levels were measured. Results MK-7 significantly increased active MGP levels compared to phytomenadione and placebo groups ( p <0.0001). No correlations were found between calcium, phosphorous, PTH, and MGP levels at baseline or after treatment. Conclusion Vitamin k supplementation was effective and tolerable in modulating MGP in hemodialysis patients, with MK-7 outperforming phytomenadione.
ISSN:2090-9098
1110-7782
2090-9098
DOI:10.1186/s43162-022-00181-1